Home NDC 80716-100 Fendall 1000 Pure Flow
Product NDC 80716-100
11-digit product format 807160100
Labeler code 80716
Product ID 80716-100_55a65211-b1c9-9b0b-e063-6294a90a5cfb
Type HUMAN OTC DRUG
Nonproprietary name Purified Water
Dosage form LIQUID
Route OPHTHALMIC
Labeler Protective Industrial Products, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-19
Substance WATER
Active strength 98.66 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Fendall 1000 Pure Flow
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 98.66 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 059QF0KO0R Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053173 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 6 of 25 · 494 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 80716-100-01 80716010001 14512.5806 g in 1 CONTAINER (80716-100-01) 14512.5806 g 2025-11-19 No No Current